Alpha-Alumina flakes having a particle thickness of 550-1000 nm, a D50-value of 15-30 μm, a D90-value of 30-45 μm and a D10-value of ≤9.0 μm. Use of the alumina flakes in varnishes, paints, automotive coatings printing inks, masterbatches, plastics and cosmetic formulations. Also, use of the alumina flakes as a substrate for effect pigments and in organic dyes.
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1. al2O3 flakes having a particle thickness of 550-1000 nm, a D50-value of 15-30 μm, a D90-value of 30-45 μm and a D10-value of ≤9.0 μm and wherein the al2O3 flakes are α-alumina flakes.
18. An assortment of al2O3 flakes having a particle thickness of 550-1000 nm, a D50-value of 15-30 μm, a D90-value of 30-45 μm and a D10-value of 9.0 μm and wherein the al2O3 flakes are α-alumina flakes.
3. The al2O3 flakes according to
4. The al2O3 flakes according to
6. The al2O3 flakes according to
7. The al2O3 flakes according to
8. The al2O3 flakes according to
9. The al2O3 flakes according to
al2O3 flake+TiO2
al2O3 flake+TiO2/Fe2O3
al2O3 flake+Fe2O3
al2O3 flake+TiO2+Fe2O3
al2O3 flake+TiO2+Fe3O4
al2O3 flake+TiO2+SiO2+TiO2
al2O3 flake+Fe2O3+SiO2+TiO2
al2O3 flake+TiO2/Fe2O3+SiO2+TiO2
al2O3 flake+TiO2+SiO2+TiO2/Fe2O3
al2O3 flake+TiO2+SiO2
al2O3 flake+TiO2+SiO2/al2O3
al2O3 flake+TiO2+al2O3
al2O3 flake+SnO2
al2O3 flake+SnO2+TiO2
al2O3 flake+SnO2+Fe2O3
al2O3 flake+SiO2
al2O3 flake+SiO2+TiO2
al2O3 flake+SiO2+TiO2/Fe2O3
al2O3 flake+SiO2+Fe2O3
al2O3 flake+SiO2+TiO2+Fe2O3
al2O3 flake+SiO2+TiO2+Fe3O4
al2O3 flake+SiO2+TiO2+SiO2+TiO2
al2O3 flake+SiO2+Fe2O3+SiO2+TiO2
al2O3 flake+SiO2+TiO2/Fe2O3+SiO2+TiO2
al2O3 flake+SiO2+TiO2+SiO2+TiO2/Fe2O3
al2O3 flake+SiO2+TiO2+SiO2
al2O3 flake+SiO2+TiO2+SiO2/al2O3
al2O3 flake+SiO2+TiO2+al2O3
al2O3 flake+TiO2+Prussian Blue or
al2O3 flake+TiO2+Carmine Red.
13. The al2O3 flakes according to
20. A composition comprising the al2O3 flakes according to
21. A formulation containing the al2O3 flakes according to
22. A formulation containing the al2O3 flakes according to
23. A process for preparing the al2O3 flakes according to
(1) preparing an aqueous solution or a slurry of at least one water-soluble and/or insoluble aluminum salt,
(2) adding an alkali solution to the aluminum salt solution to precipitate aluminum hydroxide particles, and adding a phosphorous compound and optionally at least one dopant to the aqueous solution before, during or after the precipitation,
(3) evaporating the water, followed by drying of the precipitated product of step (2) to form the dried form of alumina containing particle and alkali salt,
(4) calcining the dried form obtained in step (3) to obtain al2O3 flakes in a molten salt,
(5) removing the water soluble part of the calcined material obtained in step (4), and
(6) adjusting the particle size and thickness.
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The present invention relates to α-Al2O3 flakes and to the use thereof in paints, industrial coatings, automotive coatings, printing inks, cosmetic formulations and in particular as transparent substrate for effect pigments.
Imparting a pearlescent luster, metallic luster, color flop or multicolor effect can be achieved by using pearlescent pigments based on natural or synthetic transparent flakes. Pearlescent pigments based on α-Al2O3 flakes are well-known in the literature and commercially available under the trademark Xirallic® from Merck.
The important factors of a substrate for an effect pigment are the particle size, shape, surface property, refractive index and the like. Since large and small particles have different proportions of reflection and transmission of light on the particle surface, uniformness in particle size is essential for a vivid and uniform color. Also the particle size greatly affects the coloration of the pearlescent pigment because it is closely related with the wavelength of the light. That is, the smaller the particle size, the larger the surface area, thereby increasing the coloration and enhancing reflectivity, and offering a more vivid color. However, in coating metals or metal oxides on the surface of the Al2O3 flakes, it is usually not easy to provide uniform coatings on them and thus results in a decrease in the aspect ratio, which then reduces the effect of light interference thus deteriorating glossiness of the resulting pearlescent colors.
α-Al2O3 in the form of hexagonal flakes having a particle diameter greater than 10 μm and an aspect ratio (particle diameter/thickness) of 5-10 is known from Japanese Patent Publication No. 111239/1982.
The Japanese Patent Publication No. 72572/1991 discloses α-Al2O3 in the form of flakes having an average particle diameter of 0.5-3 μm.
The Japanese Patent Publication No. 39362/1992 describes Al2O3 in the form of fine platy particles of a hexagonal crystal system with the plane perpendicular to the c axis grown into a plate.
Al2O3 flakes composed of aluminum oxide (as a major constituent) and of titanium dioxide (as a minor constituent) are disclosed in U.S. Pat. No. 5,702,519. The Al2O3 flakes have an average particle diameter of about 5-60 μm, a thickness less than 1 μm, and an aspect ratio of >20.
WO 2006/101306 A1 and WO 2008/026829 A1 relate to zinc doped Al2O3 flakes and to pearlescent pigments based on these Al2O3 flakes. The Al2O3 flakes have an average thickness of 0.5 μm or less and an average particle diameter of ≥15 μm and a large aspect ratio (diameter/thickness) of ≥50 μm. These zinc doped Al2O3 flakes are not stable under acidic conditions and thus not suitable for all applications.
The Al2O3 flakes of the prior art have the disadvantages that they do not have a high chemical stability and/or have not the desired smoothness for the use of the flakes in cosmetic and paint applications.
The object of the present invention is to provide improved Al2O3 flakes having at the same time a high chemical stability, a smooth surface and high whiteness.
Surprisingly, it has now been found that the properties of the alumina flakes as such and of effect pigments based on alumina flakes can be increased by using alumina flakes with precisely defined dimensions and particle size distribution. Especially the optical properties of the alumina flakes and the effect pigments based on alumina flakes can be influenced by altering the particle size distribution.
Thus, the present invention relates to transparent alumina flakes which are distinguished by the fact that they have a thickness of ≥500 nm and a D90-value of 30-45 nm and a D50-value of 15-30 μm.
Compared to the prior art, the Al2O3 flakes according to the present invention show improved optical properties, in particular by their shimmer or glimmer effect combined with an increased chroma and luster and at the same time show a high chemical stability in all applications.
Since the coated and uncoated Al2O3 flakes according to the invention combine high gloss with intense interference colors and highly pronounced glitter effects, particularly effective effects can be achieved with them in various application media.
The alumina flakes according to the invention are used, in particular, as substrate for effect pigments, especially for the use in industrial applications. However, they can also be employed in all formulations where alumina flakes are usually employed, such as, for example, in inks, coatings, preferably automotive coatings, plastics, cosmetic formulations and as substrate for effect pigments.
The Al2O3 flakes of this invention have a particle size distribution characterized by a Gaussian distribution in which the volume size fractions are distributed as follows:
In this patent application D10, D50 and D90 of the alumina flakes are evaluated by using Malvern MS 2000.
The particle size distribution D50 is also known as the median diameter or the medium value of the particle size distribution, it is the value of the particle diameter at 50% in the cumulative distribution and is one of the important parameter characterizing the particle size of pigments.
Correspondingly, the D90 value indicates the maximum longitudinal dimensions of the Al2O3 flakes, as determined again by means of laser granulometry in the form of sphere equivalents, which 90% of the particles attain at maximum, or fall below, out of the entirety of all Al2O3 particles.
In a preferred embodiment, the Al2O3 flakes according to the present invention have a standard deviation of thickness distribution of less than 80, preferably 5-60 and in particular 10-50.
In a preferred embodiment the D10 value of the alumina flakes according to the present invention is <9.5, preferably ≤9.0.
The D10 value indicates the value of the longitudinal dimension of the Al2O3 flakes, as determined by means of laser granulometry in the form of the sphere equivalent, which 10% of the flakes attain at most, or fall below, out of the entirety of all the Al2O3 flakes.
The average thickness is determined on the basis of a cured paint film in which the Al2O3 flakes are oriented substantially plane-parallel to the substrate. For this purpose a transverse section of the cured paint film is examined under a scanning electron microscope (SEM), the thickness of 100 Al2O3 flakes being ascertained and statistically averaged.
The desired size and thickness distribution can be obtained by suitable classification of the flakes, such as by classifying through selected screens and the like.
The Al2O3 flakes according to the invention have a thickness of ≥500 nm, preferably 550-1000 nm, in particular 600-900 nm.
The Al2O3 flakes according to the invention preferably have an aspect ratio (diameter/thickness ratio) of 15-60, in particular of 20-45.
In a preferred embodiment the Al2O3 flakes of the present invention are α-Al2O3 flakes.
The Al2O3 flakes according to the invention can be prepared by methods known per se, as described in the literature.
In a preferred embodiment the Al2O3 flakes are prepared starting from an aqueous aluminum salt solution by precipitation with an aqueous alkali carbonate solution. An alkali metal salt like sodium or potassium sulfate and phosphoric acid or phosphate as well as a dopant like a titanium compound are added to the starting solution. The precipitation step is followed by drying (evaporation, dehydration by heating) and molten salt treatment including the following steps:
The Al2O3 flakes can be prepared by methods known per se, as described in the literature.
In a preferred embodiment the Al2O3 flakes are prepared starting from an aqueous aluminum salt solution by precipitation with an aqueous alkali carbonate solution. An alkali metal salt like sodium or potassium sulfate and phosphoric acid or and phosphate as and optionally at least one dopant, for example a titanium, zirconium, silica, indium, tin, zinc or indium compound are added to the starting solution. The precipitation step is followed by drying (evaporation, dehydration by heating), and molten salt treatment including the following steps:
Examples for suitable aluminum salts are aluminum sulfate, aluminum chloride, aluminum nitrate, poly aluminum chloride, aluminum hydroxide, boehmite, basic aluminum sulfate and combinations thereof.
Examples for suitable alkali metal salts which act as mineralizer, include sodium sulfate, potassium sulfate, lithium sulfate, magnesium sulfate, sodium chloride and potassium chloride.
The phosphoric compound is preferably selected from phosphoric acid, phosphates, diphosphoric acid, sodium phosphate, ammonium phosphate dibasic and potassium phosphate. The amount of one or more phosphorous compound(s) is preferably 0.05-2 wt. % based on the alumina flakes.
The preferred example of the pH controlling agent for the precipitation is ammonia, sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate and combinations thereof.
To control the particle size, thickness, optical properties and/or surface morphology it could be helpful to add one or more dopants in amounts of 0.01-5 wt. % based on the Al2O3 flake.
The dopant is preferably selected from the following group of compounds: TiO2, ZrO2, SiO2, In2O3, SnO2, ZnO and combinations thereof.
In a preferred embodiment the dopant is TiO2, preferably used in amounts of 0.05-3 wt. % based on the Al2O3 flakes.
The Al2O3 flakes according to the present invention are highly suitable as substrate in the preparation of effect pigments. To this end, they are preferably coated with at least one high refractive index layer, like at least one layer of a metal oxide, such as, for example, TiO2, ZrO2, SnO2, ZnO, Ce2O3, Fe2O3, Fe3O4, FeTiO5, Cr2O3, CoO, Co3O4, VO2, V2O3, NiO, furthermore of titanium suboxides (TiO2 partially reduced with oxidation states from <4 to 2, such as the lower oxides Ti3O5, Ti2O3, TiO), titanium oxynitrides, FeO(OH), thin semitransparent metal layer, for example comprising Al, Fe, Cr, Ag, Au, Pt or Pd, or combinations thereof. The TiO2 layer may be in the rutile or anatase modification. In general, the highest quality and gloss and at the same time the most stable effect pigments are obtained when the TiO2 is in the rutile modification. In order to obtain the rutile modification, an additive can be used which is able to direct the TiO2 into the rutile modification. Useful rutile directors such as tin dioxide are disclosed in the U.S. Pat. Nos. 4,038,099 and 5,433,779 and EP 0 271 767. Preferred effect pigments based on Al2O3 flakes are coated with one or more layers of metal oxides, preferably with one metal-oxide layer only, in particular with TiO2, Fe2O3, Fe3O4, SnO2, ZrO2 or Cr2O3. Especially preferred are Al2O3 flakes coated with TiO2 or Fe2O3.
The thickness of each high-refractive-index layer depends on the desired interference color. The thickness of each layer on the surface of the Al2O3 flakes is preferably 20-400 nm, preferably 30-300 nm, in particular 30-200 nm.
The number of layers on the surface of the Al2O3 flakes is preferably one or two, furthermore three, four, five, six or seven layers.
In particular, interference packages consisting of high- and low-refractive-index layers on the surface of the Al2O3 flakes result in effect pigments having increased gloss and a further increased interference color or color flop.
Suitable colorless low-refractive-index materials for coating are preferably metal oxides or the corresponding oxide hydrates, such as, for example, SiO2, Al2O3, AlO(OH), B2O3, compounds such as MgF2 or a mixture of the said metal oxides.
In case of multilayers applied on the surface of the Al2O3 flakes the interference system is, in particular, a TiO2—SiO2—TiO2 layer sequence.
Furthermore, the effect pigments according to the invention may also have a semitransparent metal layer as outer layer. Coatings of this type are known, for example, from DE 38 25 702 A1. The metal layers are preferably chromium or aluminum layers having layer thicknesses of 5-25 nm.
Al2O3 flakes can also be coated with one or more layers of a metal or metal alloy selected e.g. from chromium, nickel, silver, bismuth, copper, tin, or hastalloy. Al2O3 flakes coated with a metal sulfide are coated with sulfides e.g. of tungsten, molybdenum, cerium, lanthanum or rare earth elements.
Furthermore, the effect pigments based on Al2O3 flakes can be finally coated with an organic dye as a top coat, preferably with Prussian Blue or Carmine Red.
Particularly preferred effect pigments based on the Al2O3 flakes according to the invention have the following layer sequence(s):
The TiO2 layer(s) in the preferred embodiments mentioned above can be in the rutile or anatase modification. The Al2O3 flakes mentioned above in the preferred embodiments can be doped or undoped.
In this application, the term “coating” or “layer” is taken to mean the complete enveloping of the Al2O3 flakes according to the invention.
The effect pigments based on doped or undoped Al2O3 flakes preferably consist of 40-90 wt. % of Al2O3 flakes and 10-60 wt. % of the coating based on the total pigment.
The Al2O3 flakes can be coated by wet chemical coating, by CVD or PVD processes.
The coating of the α-Al2O3 flakes with one or more layers, preferably one or more metal oxide layers, is preferably carried out by wet-chemical methods, it being possible to use the wet-chemical coating methods developed for the preparation of pearlescent pigments. Methods of this type are described, for example, in DE 14 67 468, DE 19 59 988, DE 20 09 566, DE 22 14 545, DE 22 15 191, DE 22 44 298, DE 23 13 331, DE 15 22 572, DE 31 37 808, DE 31 37 809, DE 31 51 343, DE 31 51 354, DE 31 51 355, DE 32 11 602, DE 32 35 017 or also in further patent documents and other publications known to the person skilled in the art.
In the case of wet coating, the Al2O3 flakes are suspended in water, and one or more hydrolysable metal salts are added at a pH which is suitable for hydrolysis, which is selected in such a way that the metal oxides or metal-oxide hydrates are precipitated directly onto the flakes without secondary precipitations occurring. The pH is usually kept constant by simultaneous metered addition of a base and/or acid. The pigments are subsequently separated off, washed and dried at 50-150° C. for 6-18 h and calcined for 0.5-3 h, where the calcination temperature can be optimised with respect to the respective coating present. In general, the calcination temperatures are 500-1000° C., preferably 600-900° C. If desired, the pigments can be separated off after application of individual coatings, dried and optionally calcined and then re-suspended again for the application of the further layers.
The application of a SiO2 layer to the Al2O3 flake and/or to the already coated Al2O3 flake is generally carried out by addition of a potassium or sodium water-glass solution at a suitable pH.
Furthermore, the coating can also be carried out in a fluidised-bed reactor by gas-phase coating, it being possible to use, for example, the methods proposed in EP 0 045 851 and EP 0 106 235 for the preparation of pearlescent pigments correspondingly.
The hue and chroma of the effect pigment based on Al2O3 flakes according to the invention can be varied in very broad limits through the different choice of the coating amounts or the layer thicknesses resulting therefrom. Fine tuning for a certain hue and chroma can be achieved beyond the pure choice of amount by approaching the desired color under visual or measurement technology control.
In order to increase the light, water and weather stability, it is frequently advisable, depending on the area of application, to subject the finished pigment to post-coating or post-treatment. Suitable post-coatings or post-treatments are, for example, the processes described in DE 22 15 191 C2, DE-A 31 51 354, DE-A 32 35 017 or DE-A 33 34 598. This post-coating further increases the chemical and photochemical stability or simplifies the handling of the pigment, in particular the incorporation into various media. In order to improve the weatherability, dispersibility and/or compatibility with the user media, it is possible, for example, for functional coatings of Al2O3 or ZrO2 or mixtures thereof to be applied to the pigment surface. Furthermore, organic post-coatings are possible, for example with silanes, as described, for example, in EP 0090259, EP 0 634 459, WO 99/57204, WO 96/32446, WO 99/57204, U.S. Pat. Nos. 5,759,255, 5,571,851, WO 01/92425 or in J. J. Ponjeé, Philips Technical Review, Vol. 44, No. 3, 81 ff. and P. H. Harding J. C. Berg, J. Adhesion Sci. Technol. Vol. 11 No. 4, pp. 471-493.
In accordance with the present invention, an effect pigment based on Al2O3 flakes having the desired size distribution has been found useful in all types of compositions, including plastics, cosmetics, and, in particular in automotive paints.
The Al2O3 flakes and the effect pigments based on Al2O3 flakes according to the invention are compatible with a multiplicity of color systems, preferably from the area of paints, automotive coatings, industrial coatings, and printing inks and cosmetic formulations. For the preparation of printing inks for, for example, gravure printing, flexographic printing, offset printing and offset overvarnishing, a multiplicity of binders, in particular water-soluble grades, as sold, for example, by BASF, Marabu, Pröll, Sericol, Hartmann, Gebr. Schmidt, Sicpa, Aarberg, Siegberg, GSB-Wahl, Follmann, Ruco or Coates Screen INKS GmbH, is suitable. The printing inks can be water-based or solvent-based. The Al2O3 flakes and the effect pigments according to the invention are furthermore also suitable for the laser marking of paper and plastics and for applications in the agricultural sector, for example for greenhouse sheeting, and, for example, for the coloring of tent awnings.
It goes without saying that, for the various applications, the coated and uncoated Al2O3 flakes according to the present invention can also advantageously be used in blends with organic dyes, organic pigments or other pigments, such as, for example, transparent and opaque white, colored and black pigments, and with flake-form iron oxides, organic pigments, holographic pigments, LCPs (liquid crystal polymers) and conventional transparent, colored and black luster pigments based on metal oxide-coated mica and SiO2 flakes, etc. The pigments according to the invention can be mixed in any ratio with commercially available pigments and fillers.
Fillers which may be mentioned are, for example, natural and synthetic mica, nylon powder, pure or filled melamine resins, talc, SiO2, glasses, kaolin, oxides or hydroxides of aluminum, magnesium, calcium or zinc, BiOCl, barium sulfate, calcium sulfate, calcium carbonate, magnesium carbonate, carbon, and physical or chemical combinations of these substances. There are no restrictions regarding the particle shape of the filler. It can be, for example, flake-form, spherical or needle-shaped in accordance with requirements.
The Al2O3 flakes and the effect pigments based on Al2O3 flakes according to the invention are simple and easy to handle. The Al2O3 flakes and the effect pigments based on Al2O3 flakes can be incorporated into the system in which it is used by simple stirring. Laborious milling and dispersing of the Al2O3 flakes and the effect pigments is not necessary.
The Al2O3 flakes and the effect pigments based on Al2O3 flakes according to the invention can be used for pigmenting coating materials, printing inks, plastics, agricultural films, button pastes, for the coating of seed, for the coloring of food, coatings of medicaments or cosmetic formulations. The concentration of the Al2O3 flakes and the effect pigments in the system in which it is to be used for pigmenting is generally between 0.01 and 50% by weight, preferably between 0.1 and 5% by weight, based on the overall solids content of the system. This concentration is generally dependent on the specific application.
Plastics containing the Al2O3 flakes and the effect pigments based on Al2O3 flakes according to the invention in amounts of 0.1 to 50% by weight, in particular from 0.5 to 7% by weight, are frequently notable for a particular gloss and shimmer effect.
In the coating sector, especially in automotive coating and automotive finishing, the effect pigments based on Al2O3 flakes according to the invention are employed in amounts of 0.5-10% by weight.
In the coating material, the Al2O3 flakes and the effect pigments based on Al2O3 flakes according to the invention have the advantage that the desired color and gloss is obtained by a single-layer coating (one-coat systems or as a base coat in a two-coat system).
In the pigmentation of binder systems, for example for paints and printing inks for intaglio, offset or screen printing, the effect pigments based on Al2O3 flakes with Stapa®-aluminum and gold bronze pastes from Eckart GmbH have proven particularly suitable. The effect pigment is incorporated into the printing ink in amounts of 2-50% by weight, preferably 5-30% by weight and, in particular, 8-15% by weight. The printing inks containing the effect pigment according to the invention in combination with a metal effect pigment exhibits purer hues and is of improved printability owing to the good viscosity values.
The invention likewise provides pigment preparations containing coated or uncoated Al2O3 flakes according to the present invention and further effect pigments, binders and, if desired, additives, the said preparations being in the form of substantially solvent-free, free-flowing granules. Such granules contain up to 95% by weight of the Al2O3 flakes or the effect pigments according to the invention. A pigment preparation in which the effect pigment based on Al2O3 flakes of the invention is pasted up with a binder and with water and/or an organic solvent, with or without additives, and the paste is subsequently dried and brought into a compact particulate form, e.g. granules, pellets, briquettes, a masterbatch or tablets, is particularly suitable as a precursor for printing inks.
The invention thus also relates to the use of the coated (=effect pigments) or uncoated Al2O3 flakes in formulations from the areas of paints, coatings, automobile coatings, automotive finishing, industrial coatings, paints, powder coatings, printing inks, security printing inks, plastics, ceramic materials, cosmetics. The coated and uncoated Al2O3 flakes can furthermore be employed in glasses, in paper, in paper coating, in toners for electrophotographic printing processes, in seed, in greenhouse sheeting and tarpaulins, in thermally conductive, self-supporting, electrically insulating, flexible sheets for the insulation of machines or devices, as absorber in the laser marking of paper and plastics, as absorber in the laser welding of plastics, in pigment pastes with water, organic and/or aqueous solvents, in pigment preparations and dry preparations, such as, for example, granules, for example in clear coats in the industrial and automobile sectors, in sunscreens, as filler, in particular in automobile coatings and automotive finishing.
All percentage data in this application are percent by weight, unless indicated otherwise.
The following examples are intended to explain the invention in greater detail, but without restricting it. Above and below, all percentages are percent by weight.
In 300 ml of deionized water are dissolved 111.9 g of aluminum sulfate 18-hydrate, 57.3 g of anhydrous sodium sulfate, and 46.9 g of potassium sulfate by heating above 60° C. To the resulting solution is added 1.0 g of 34.4% solution of titanyl sulfate. The resulting solution is designated as the aqueous solution (a).
In 150 ml of deionized water are 0.45 g of sodium tertiary phosphate 12-hydrate and 54.0 g of sodium carbonate. The resulting solution is designated as the aqueous solution (b).
The aqueous solution (b) is added with stirring to the aqueous solution (a) kept at about 60° C. Stirring is continued for 15 minutes. The resulting mixture of the two solutions is a gel. This gel is evaporated to dryness, and the dried product is heated at 1200° C. for 5 hours. Water is added to the heated product to dissolve free sulfate. Insoluble solids are filtered off, washed with water, and finally dried. The obtained alumina flake is examined by X-ray diffractometry. The diffraction pattern has only peaks attributed to corundum structure (α-alumina structure).
D50 is 13.0 μm and D90 is 22.0 μm and the thickness is 200 nm.
74.6 g of aluminum sulfate 18-hydrate, 5.7 g of transition alumina (C10W: Nippon Light Metal Co., Ltd.), 57.3 g of anhydrous sodium sulfate and 46.9 g of potassium sulfate are dissolved in 450 ml of deionized water by heating above 60° C. To the resulting solution is added 1.2 g of 34.4 solution of titanyl sulfate. The resulting solution is designated as the aqueous solution (a).
In 300 ml of deionized water are 0.010 g of sodium tertiary phosphate 12-hydrate and 55.0 g of sodium carbonate. The resulting solution is designated as the aqueous solution (b).
The aqueous solution (b) is added with stirring to the aqueous solution (a) kept at about 60° C. Stirring is continued for 30 minutes. The resulting mixture of the two solutions is a slurry. This slurry is evaporated to dryness, and the dried product is heated at 1230° C. for 4.5 hours. Water is added to the heated product to dissolve free sulfate. Insoluble solids are filtered off, washed with water, and filtered by sieve with 25 micron opening. And finally it was dried. The obtained alumina flake is examined by X-ray diffractometry. The diffraction pattern have only peaks attributed to corundum structure (α-alumina structure).
D50 is 19.6 μm, D90 is 38.8 μm and the average thickness is 700 nm.
20 g of alumina flakes of Comparative Example 1 are suspended in 400 ml of deionized water. To the resulting suspension (kept at about 65° C.) is added a solution containing 125 g of TiCl4 per liter. Simultaneously a 10 solution of NaOH was added to keep the pH at 2.1. The addition of the TiCl4 solution is stopped when the resulting product takes on a silvery color. The suspending solids are filtered off, washed with water and dried. Finally, the dried solids are calcined at 850° C. for 30 minutes to give a whitish and a little glossy pearlescent pigment.
20 g of alumina flakes of Example 1 are suspended in 400 ml of deionized water. To the resulting suspension (kept at about 65° C.) is added a solution containing 125 g of TiCl4 per liter. Simultaneously a 10% solution of NaOH was added to keep the pH at 2.1. The addition of the TiCl4 solution is stopped when the resulting product takes on a silvery color. The suspending solids are filtered off, washed with water and dried. Finally, the dried solids are calcined at 850° C. for 30 minutes to give a highly whitish and glossy pearlescent pigment with a strong glitter effect.
20 g alumina flakes of Comparative Example 1 are suspended in 400 ml of deionized water. To the resulting suspension (kept at about 75° C.) are added a solution containing 300 g of FeCl3 per liter. Simultaneously a 10 solution of NaOH was added to keep the pH at 3.0. The addition of the FeCl3 solution was stopped when the resulting product takes on a most reddish color. The suspending solids are filtered off, washed with water, and dried. Finally, the dried solids are calcined at 800° C. for 30 minutes to give a moderate luster and brownish red colored pearlescent pigment.
20 g alumina flakes of Example 1 are suspended in 400 ml of deionized water. To the resulting suspension (kept at about 75° C.) are added a solution containing 300 g of FeCl3 per liter. Simultaneously a 10% solution of NaOH was added to keep the pH at 3.0. The addition of the FeCl3 solution was stopped when the resulting product takes on a most reddish color. The suspending solids are filtered off, washed with water, and dried. Finally, the dried solids are calcined at 800° C. for 30 minutes to give a high luster and pure red colored pearlescent pigment with a strong glitter effect.
20 g alumina flakes of Comparative Example 1 are suspended in 400 ml of deionized water. To the resulting suspension (kept at about 65° C.) is added a solution containing 50 g of SnCl4 per liter. Simultaneously a 10% solution of NaOH is added to keep the pH at 2.1 until the total adding volume of SnCl4 solution become 17 ml. Next the solution containing 125 g of TiCl4 per liter was added to the resulting suspension. Simultaneously a 10% solution of NaOH is added to keep the pH at 2.1. The addition of the TiCl4 solution is stopped when the resulting product takes on a silvery color. The suspending solids are filtered off, washed with water, and dried. Finally, the dried solids are calcined at 850° C. for 30 minutes to give a whitish and a little glossy pearlescent pigment.
20 g alumina flakes of Example 1 are suspended in 400 ml of deionized water. To the resulting suspension (kept at about 65° C.) is added a solution containing 50 g of SnCl4 per liter. Simultaneously a 10% solution of NaOH is added to keep the pH at 2.1 until the total adding volume of SnCl4 solution become 17 ml. Next the solution containing 125 g of TiCl4 per liter was added to the resulting suspension. Simultaneously a 10% solution of NaOH is added to keep the pH at 2.1. The addition of the TiCl4 solution is stopped when the resulting product takes on a silvery color. The suspending solids are filtered off, washed with water, and dried. Finally, the dried solids are calcined at 850° C. for 30 minutes to give a highly whitish and highly glossy pearlescent pigment with a strong glitter effect. At the luster angle, the glossy appearance can be seen at a more wider angle compared to Comparative Example 1.3.
20 g alumina flakes of Comparative Example 1 are suspended in 400 ml of deionized water. To the resulting suspension (kept at about 65° C.) is added a solution containing 125 g of TiCl4 per liter. Simultaneously a 10% solution of NaOH is added to keep the pH at 2.1. The addition of the TiCl4 solution is stopped when the resulting product takes on a yellowish color. Then a solution containing 50 g of Na2SiO3 per liter is added to the resulted suspension. Simultaneously a 10% solution of HCl is added to keep the pH at 7. Next a solution containing 125 g of TiCl4 per liter is added to the resulted suspension. Simultaneously a 10% solution of NaOH is added to keep the pH at 2.1. The addition of the TiCl4 solution is stopped when the resulting product takes on a bluish color. The suspending solids are filtered off, washed with water, and dried. Finally, the dried solids are calcined at 850° C. for 30 minutes to give a blue-whitish and a little glossy pearlescent pigment.
20 g alumina flakes of Example 1 are suspended in 400 ml of deionized water. To the resulting suspension (kept at about 65° C.) is added a solution containing 125 g of TiCl4 per liter. Simultaneously a 10% solution of NaOH is added to keep the pH at 2.1. The addition of the TiCl4 solution is stopped when the resulting product takes on a yellowish color. Then a solution containing 50 g of Na2SiO3 per liter is added to the resulted suspension. Simultaneously a 10% solution of HCl is added to keep the pH at 7. Next a solution containing 125 g of TiCl4 per liter is added to the resulted suspension. Simultaneously a 10% solution of NaOH is added to keep the pH at 2.1. The addition of the TiCl4 solution is stopped when the resulting product takes on a bluish color. The suspending solids are filtered off, washed with water, and dried. Finally, the dried solids are calcined at 850° C. for 30 minutes to give a highly bluish and highly glossy pearlescent pigment with a strong glitter effect. At the luster angle, the stronger bluish color and higher glossy appearance can be seen at a more wider angle compared to Comparative Example 1.4.
Measurements
Evaluation for Particle Size D10, D50 and D90
D10, D50 and D90 of alumina flake are evaluated by using Malvern MS2000.
Determination of the Thickness and Particle Size and the Thickness Distribution
0.01 g/l of the alumina flake slurry is prepared and 0.1 ml of this slurry is dropped onto a flat substrate like a silicon wafer. The substrate is dried and cut to adequate size. The substrate is set with almost vertically tilted angle on the base of SEM (Scanning electronic microscope) and the thickness of the alumina flake is determined.
The thickness of more than 100 alumina flakes is measured for the calculation of the thickness distribution. The standard deviation of the thickness is calculated with the Gaussian distribution equation.
Preparation for a Sprayed Panel
A base coat paint for automobiles is prepared according to the following formulation.
<Base coat system> Acrylic-melamine resin system
“Acrydic ® 47-712”*
70 pbw
“Superbekkamine ® G821-60”**
30 pbw
Toluene
30 pbw
Ethyl acetate
50 pbw
*Acrylic resin from Dainippon Ink & Chemicals, Inc.
**Melamine resin from Dainippon Ink & Chemicals, Inc.
<Base coat system> Acrylic-melamine resin system
n-Butanol
110 pbw
Solvesso ® #150
40 pbw
The above acrylic-melamine resin system (100 pbw) is incorporated with 20 pbw of the pearlescent pigment according to one of the above given Examples. The resulting compound is diluted with a thinner so that the resulting paint has an adequate consistency for spraying (12-15 seconds, for cup #4). This paint is applied to a substrate by spraying to form a base coat layer.
The base coated layer is coated further with a colorless top clear coat paint, which is prepared according to the following formulation.
<Top Clear Coat System>
<Top clear coat system>
“Acrydic ® 47-712”
14 pbw
“Superbekkamine ® L117-60”
6 pbw
Toluene
4 pbw
MIBK
4 pbw
Butyl cellosolve
3 pbw
The top clear coating is exposed to air at 40° C. for 30 minutes and then cured at 135° C. for 30 minutes.
Haze-gloss (BYK) is the analyzing equipment to evaluate luster and haze. In this patent application, the value of mirror gloss on 60° is measured by Haze-gloss and represents the value of the luster. Compared to the prior art the coated Al2O3 flakes show very high values for the luster. High luster values are necessary to achieve a good appearance in the applications. The haze values measured by this equipment are affected by spreading of the reflection angle. In this patent application, the wider spreading angle is important for the pearlescent appearance. The coated Al2O3 flakes according to the present invention show very high haze-gloss values. To differentiate the evaluation result, panels are used which are sprayed with a base coat before they are coated with a top clear coat for the haze-gloss measurement.
Wave-scan dual (BYK) is used as the analyzing equipment to measure the surface flatness of the samples. Wa value represents the cyclic flatness in the range of 0.1-0.3 mm. A smaller value in this patent application represents a flatter surface showing the advantages of the pigments according to the present invention.
Sprayed panels with a top clear coat are measured for Wa. Flatter surfaces have better finishing appearance.
BYK-mac is used to evaluate glitter effect. The SG value represents the glitter.
Wave-scan dual (BYK) is used to evaluate the finishing quality of paint.
The optical properties of the pearlescent pigments according to the above given examples are summarized in the following table:
TABLE 1
Optical
TiO2
Particle size
Average
properties of
coated
distribution of the
thickness of
TiO2 coated
Al2O3
Al2O3
Al2O3 flakes (μm)
the Al2O3 flakes
Al2O3 flakes
flakes
flakes
D10
D50
D90
(nm)
SG
Wa
E1
E1.1
9.0
19.6
38.8
700
8.5
13
CE1
CE1.1
4.8
13.0
22.0
200
2
21
The entire disclosures of all applications, patents and publications, cited herein and of corresponding European Application No. 13002294.0, filed Apr. 30, 2013 are incorporated by reference herein.
Pfaff, Gerhard, Nitta, Katsuhisa, Schoen, Sabine, Kobayashi, Satoru, Takenaka, Yuji, Suzuki, Ryuta, Sasaki, Fumiko, Kunii, Koshiro
| Patent | Priority | Assignee | Title |
| Patent | Priority | Assignee | Title |
| 5702519, | Sep 14 1995 | Merck Patent Gesellschaft mit ceschrankter Haftung | Flaky aluminum oxide and pearlescent pigment, and production thereof |
| 6197277, | Aug 24 1995 | KINSEI MATEC CO , LTD | Process for producing alumina particles having high dispersibility and plasticity |
| 6306788, | Jan 29 1999 | Sumitomo Chemical Company, Limited | Translucent alumina sintered body and production thereof |
| 6596070, | Oct 17 1997 | Merck Patent Gesellschaft | Interference pigments |
| 7067157, | Apr 17 2000 | KINSEI MATEC CO , LTD | Flaky α-alumina particles and method for producing the same |
| 7959894, | Mar 25 2005 | Korea Research Institute of Chemical Technology; CQV CO , LTD | Flaky alpha-alumina crystal and a method of its preparation |
| 7993746, | Aug 28 2006 | Korea Research Institute of Chemical Technology; CQV CO , LTD | Flaky alpha-alumina crystals with large aspect ratio and a preparation method of the same |
| 8088212, | Apr 01 2005 | BASF COLORS & EFFECTS USA LLC; Sun Chemical Corporation; BASF Corporation | Sparkle effect of unique particle size distribution |
| 8287636, | Aug 28 2006 | Korea Research Institute of Chemical Technology; CQV CO , LTD | Pearlescent pigments with large aspect ratio and a method of their preparation |
| 9683105, | Dec 09 2011 | NIPPON SHEET GLASS COMPANY, LIMITED | Photoluminescent pigment, and photoluminescent paint composition and automobile outer panel coating material containing same |
| 9909010, | Dec 20 2012 | Merck Patent GmbH | Pigments |
| 20010043910, | |||
| 20030097965, | |||
| 20040265507, | |||
| 20060027141, | |||
| 20060053975, | |||
| 20060223910, | |||
| 20090186225, | |||
| 20090320719, | |||
| 20100015445, | |||
| 20100297045, | |||
| 20110031640, | |||
| 20110052485, | |||
| 20110226161, | |||
| 20110237683, | |||
| 20140335348, | |||
| 20140349009, | |||
| CN101189306, | |||
| CN101541681, | |||
| CN101965383, | |||
| CN102741358, | |||
| CN1263877, | |||
| CN1513039, | |||
| EP1148028, | |||
| EP2799398, | |||
| JP2008534753, | |||
| JP2010502539, | |||
| JP2010502774, | |||
| WO2006101306, | |||
| WO2006110359, | |||
| WO2008026829, | |||
| WO2008026860, | |||
| WO2009103322, | |||
| WO2013085049, | |||
| WO2014094993, |
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